Analytical Development Technician

Chemo; Azuqueca de Henares; Presencial; EUR 45.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Salary package

Company cafeteria

Benefits program

Development plans

Descripción de la vacante

Insud Pharma seeks an Analytical Development Scientist to join its team in Spain, focusing on developing, validating and transferring robust analytical methods for injectable products and raw materials. You will coordinate internal and CRO activities, ensuring compliance with GMP and regulatory timelines.

The role requires 3–5 years of pharma experience, expertise in LC/UPLC and MS, and strong English/Spanish communication. Attractive salary and career development opportunities are offered.

Formación

• 3–5 years of experience in analytical development in pharma
• Experience with LC/UPLC, GC, SEC and MS
• GMP, ICH, FDA and USP/EP knowledge
• Strong English and Spanish writing skills

Responsabilidades

• Develop, validate, and transfer analytical methods for injectable formulations and raw materials
• Support formulation development, stability testing, and QC activities
• Coordinate internal and CRO analyses in Spain and abroad
• Prepare analytical protocols, specifications, reports, and bulletins
• Oversee method transfer to QC laboratories
• Review data and reports across departments and partners

Conocimientos

Analytical method development

LC/UPLC

Mass spectrometry

GMP/ICH regulations

Technical writing

Educación

MSc in Analytical Chemistry or Pharmacy degree

Herramientas

HPLC/UPLC

Descripción del empleo

Experience: 3 to 5 years in similar roles.

What are we looking for?

We are looking for an Analytical Development Scientist to join our team and support the development of injectable drug products. In this role, you will be responsible for developing, validating, and transferring robust analytical methods for formulations and raw materials, ensuring compliance with project timelines, GMP standards, and regulatory requirements. You will play a key role in supporting formulation development, stability studies, quality control activities, and analytical investigations, while coordinating internal and external analytical work performed by CROs and partner laborator

The challenge!

• Develop, optimize, validate, and transfer analytical methods for injectable drug product formulations and raw materials.
• Support formulation development, stability testing, and quality control activities through reliable and robust analytical methodologies
• Coordinate and follow up analytical development, validation, and transfer activities performed internally or outsourced to CROs in Spain and other countries
• Ensure successful analytical method transfer to Quality Control laboratories.
• Perform analytical investigations and troubleshooting to support development, validation, and transfer activities
• Write and review analytical protocols, specifications, reports, and work bulletins.
• Evaluate analytical results and coordinate laboratory analysts’ activities.
• Review and report analytical work performed by other departments, group companies, and external third parties.
• Prepare analytical documentation to support regulatory and clinical activities.
• Manage verification and testing methods for raw materials in line with project deadlines.
• Coordinate and review the work carried out in the Analytical Development Laborlines.
• Oversee Analytical Development Laboratory equipment management.

Specific Knowledge:

• Strong knowledge of analytical instrumentation
• Solid expertise in chromatography techniques: LC, GC, and SEC.Good experience with Mass Spectrometry (MS).Sound knowledge of GMP, ICH, FDA, and USP/EP pharmacopeias
• Good spoken English and very strong written communication skills in English and Spanish fluency

Experience (years/area):

• At least 3 years of experience as an Analytical Development Scientist in the pharmaceutical in Industry at least 3 years of hands-on experience in Liquid Chromatography, within a GMP environment. Strong experience with HPLC; UPLC is considered
• Experience in the characterization of parenteral depot formulations is a a plus.
• Expertise in USP Type IV dissolution apparatus is a plus.
• EducationMSc in Analytical Chemistry or a related scientific discipline with strong chemistry content, or Pharmacy degree with relevant professional experience in analytical development.

Flexible start hours from Monday to Friday (full 40-hour

workweek).

Attractive salary package.

Company cafeteria (free of charge).

Benefits and Savings Club.

Development plans, internal mobility policy.

How will the Selection Process be?

Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these two channels.

Prepare well! We will continue with a face-to-face/virtual interview based on availability and as agreed; there may be one or two interviews, and depending on the type of process, there may also be some kind of test.

Wait for the result! We care that you feel guided and know what to expect from us at every step of the selection process, so we will always try to inform you about the status of the process.

Do you think this offer is not

for you?

The Insud Pharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as established in current regulations - Organic Law 3/2007, and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.